Regulatory affairs courses, webinars, conferences and meetings

We offer a comprehensive programme of training courses, conferences, meetings and webinars on a wide range of regulatory affairs topics.

Our courses are delivered by highly regarded experts from industry and government agencies and are suitable for professionals at all stages of their regulatory career. Read more about the different regulatory affairs course categories and how these relate to your own career.

Our commitment to quality

TOPRA is proud to have provided gold standard training for regulatory affairs professionals for more than 40 years. Our commitment to the profession, to everyone who attends our training and to employers who entrust their staff development to us, is given in our Quality Statement.

Download TOPRA's Courses & Conferences calendar for 2021 (PDF)

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10/05/2021CRED US Regulation of MedicinesThis CRED course is designed for regulatory affairs professionals with some knowledge and experience of other markets to gain an understanding of the key principles and requirements for US approval of a medicine. OnlineUSREG21
11/05/2021TOPRA In Ireland - Overview of PRRCRegister for this TOPRA In Ireland webinar to gain further insight into the role of the Person Responsible for Regulatory Compliance (PRRC) from ex NB Technical Expert, Richard Tully, on his expectations and advice to manufacturers as application deadline approaches. OnlineIREMAY21
11/05/2021The Regulatory Environment of Medicines in South AfricaThis webinar will provide the attendee with a high-level operational understanding of the medicine and related products regulatory landscape in South Africa and Southern Africa, with a focus on well-regulated, Anglophone countries. OnlineWEBMEDSA
12/05/2021CRED Successful and Skilful CommunicationSkilful communication and negotiation skills are essential for effective regulatory professionals. Learn to recognise and use different negotiation strategies whilst maintaining trust and respect with complex groups of stakeholders. Develop and deliver impactful presentations and documents that deliver the results you need. OnlineCOMM211
12/05/2021Biotech SPIN: Fast To Market PathwaysTOPRA's Biotech SPIN present a webinar on "Fast to market pathways for clinical development in the US and EU", presented by Jayne Hunt, MTOPRA and Kate Parsley, Director of Regulatory Affairs for Gyroscope Therapeutics, UK. OnlineBIOMAY21
18/05/2021TOPRA NA- Ad Promo Submissions: Preparing for ECTD MandateThe TOPRA IN North America Network is delighted to announce the upcoming webinar on Ad Promo Submissions: Preparing for the eCTD Mandate, presented by Allison Steffen, Regulatory Operations, WAYS Pharmaceutical Services. OnlineNAMAY21
19/05/2021Regulatory Careers Live 2021 - Webinar DayRegulatory Careers Live is your opportunity to meet with potential future employers and get essential advice from some of the most respected and influential leaders in the field of regulatory affairs. OnlineRCL21WEB
20/05/2021TOPRA Summit 2021Focusing on the changes and disruptions that COVID-19 has brought, this year's Summit will look at the new norm and where we should go from here. OnlineSUMMIT21
24/05/2021TOPRA In Sweden - Regulatory Update and Covid 19 MeetingThis evening is an ideal opportunity to hear the latest regulatory news on Pharmaceuticals and Medical Devices. We will also talk about how Covid-19 has influenced the work within MPA and industry and some TOPRA news. Björn Eriksson, new Director General at MPA since March 2021 will visit us. Event online due to covid-19 meeting restrictions at MPA. SwedenMPA2OO
26/05/2021CRED Managing Lifecycle and Variations EffectivelyRegulatory professionals in industry and agencies spend a significant amount of time on variations, so getting them right is critical. OnlineVAR21
01/06/2021Regulation of In Vitro Diagnostics Medical DevicesModule 19 of the MSc and Masterclass: Primarily focusing on the In Vitro Diagnostic Regulation, this course will present the latest information covering the new regulation and how this differs from the In Vitro Diagnostic Directive in the EU and other jurisdictions.LondonUnited KingdomMC192021
01/06/2021Regulation of In Vitro Diagnostic Medical DevicesModule 19 of the MSc and Masterclass: Primarily focusing on the In Vitro Diagnostic Regulation, this course will present the latest information covering the new regulation and how this differs from the In Vitro Diagnostic Directive in the EU and other jurisdictions. OnlineMC1920210
09/06/2021CRED Project Management for Regulatory Affairs ProfessionalsA two-day, skills-based course on the theory and practice of managing project teams to produce optimal regulatory documents and communications for those working in the pharmaceutical industry. OnlinePM21
11/06/2021CRED An Overview of Regulatory Product InformationThis one day workshop from regulators and industry experts will provide an insight on European SmPC, package leaflet (PL) and label preparation and implementation, from a strategic and practical point of view.LondonUnited KingdomSMPC21
11/06/2021CRED An Overview of Regulatory Product InformationThis one day workshop from regulators and industry experts will provide an insight on European SmPC, package leaflet (PL) and label preparation and implementation, from a strategic and practical point of view. OnlineSMPC21VIR
14/06/2021Essentials of European Regulatory Affairs, United StatesThis course will provide you with the opportunity to learn about European Regulatory Affairs direct from the source. OnlineBASUS0621
23/06/2021Compiling Successful Clinical Trial ApplicationsThis online course will equip you with the key knowledge on clinical trials applications you need as a regulatory professional. OnlineCT21
23/06/2021Compiling Successful Clinical Trial ApplicationsThis face-to-face course will equip you with the key knowledge on Clinical Trials applications you need as a regulatory professional.LondonUnited KingdomCT21F2F
30/06/2021Strategic Planning in Regulatory AffairsMasterclass and Module 1 of the MSc: This Masterclass will help you understand the practical and strategic aspects of global regulatory affairs, and enable you to develop your knowledge and skills to provide advice to your company to help develop a regulatory strategy.OnlineOnlineMSCM12021O
07/07/2021The Medical Device Introductory CourseModule 13 of the MSc and Masterclass (Principles of Medical Device Regulatory Affairs): Providing those new to Medical Device Regulatory Affairs with an understanding of the regulatory requirements for medical devices in the EU.WatfordUnited KingdomINTROMD21
01/08/2021PhD Annual Registration Fee 2021   PHDREG2018
01/08/2021PhD Annual Registration Fee   PHDREG2019
01/08/2021PhD Annual Registration Fee 2020/2021   PHDREG2021
05/08/2021Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.LondonUnited KingdomBAS0508
06/09/2021Regulatory Requirements for Cell, Tissue and Gene TherapiesModule 22 of the MSc and Masterclass: Designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation of advanced therapy medicinal products, which has grown in significance over the past five years. It fills a gap in the educational needs for contemporary regulatory affairs specialists. It will allow students to examine the regulatory requirements for advanced therapy medicinal products in the EU and compare this with other territories. It will consider the scientific principles underpinning the development and regulation of advanced therapy medicinal products and the complexities involved.LondonUnited KingdomMSCM222021
22/09/2021Human Medicines Symposium 2021Speakers from agencies across Europe will provide a broad range of insight and facilitate discussion into the world of regulatory affairs on matters affecting industry professionals today and in the future.PragueCzech RepublicHSYM2021
22/09/2021TOPRA Annual Symposium Exhibitor Package 2021A truly unique and valuable event in regulatory affairs, TOPRA Symposium is the only conference in Europe entirely focused on healthcare regulatory affairs, allowing you to meet a closely defined group of professionals.PragueCzech RepublicSYMEXHIB21
22/09/2021Human Medicines Symposium 2021 (Online)The TOPRA Symposium brings together regulators, experts and thought leaders in this global conference dedicated to discussing the latest insights into the world of regulatory affairs. OnlineVHUMSYM21
22/09/2021Veterinary Medicines Symposium 2021The Veterinary Medicines Symposium will concentrate on how we can improve animal health with veterinary medicines by looking at how we collaborate now and in the future, what strategies could be put in place and how we can work together towards new solutions.PragueCzech RepublicVSYM2021
22/09/2021Veterinary Medicines Symposium 2021 (Online)The Veterinary Medicines Symposium will concentrate on how we can improve animal health with veterinary medicines by looking at how we collaborate now and in the future, what strategies could be put in place and how we can work together towards new solutions. OnlineVVETSYM21